D ermatophytosis caused byTrichophyton rubrum is the most common cutaneous fungal infection worldwide (1), which represents the cause of between 80% and 90% of all chronic and recurrent infections (2). These infections establish an important public health problem because of the prolonged treatment required for the disease, because of the frequent recurrence of infection, and because they are generally considered difficult to manage (3). Reliable in vitro susceptibility testing would therefore be useful for selecting the most suitable antifungal treatment. For many years, griseofulvin was the only approved systemic antidermatophytic agent (4). However, nowadays, many potent antifungal agents are available for the treatment of dermatophytosis, such as allylamines and triazoles, which have more potent activity and fewer side effects (5-19). The expansion of information on in vitro susceptibility testing of dermatophytes to new antifungal agents will help in the selection and development of antifungal drug regimens.The aim of the current study was to compare in vitro the activities of three newer triazoles, voriconazole, posaconazole, and isavuconazole, and four established antifungal agents against T. rubrum infection. One hundred eleven clinical isolates of T. rubrum were collected from seven dermatology clinics in Shanghai, China. Morphological identifications were confirmed by sequence-based analysis of the internal transcribed spacer of the rRNA gene region. The in vitro activities of seven antifungal agents were determined according to the CLSI reference guideline M38-A2 (20), with minor modifications. Two reference strains, Trichophyton mentagrophytes (strain ATCC MYA-4439) and Candida parapsilosis (strain ATCC 22019), were included as quality controls. Student's t test with the statistical SPSS package (version 9.0) was used, and P values of Ͻ0.05 were considered statistically significant. Table 1 lists the MIC ranges, geometric mean (GM) MICs, MIC 50 s, and MIC 90 s of seven antifungal agents against 111 T. rubrum strains. Terbinafine, voriconazole, posaconazole, isavuconazole, itraconazole, and griseofulvin had low MICs against all tested strains, whereas fluconazole did not show inhibitory effects. Similar results have been achieved in other studies (Table 2); however, limited data are available for the newer triazoles isavuconazole and posaconazole.Terbinafine was one of the most effective antifungal agents against T. rubrum among the 7 fungal agents tested, and our findings confirm those of previous studies (5-19) ( Table 2). We compared the in vitro activities of the 3 newer triazoles isavuconazole, posaconazole, and voriconazole with that of itraconazole. Three newer triazoles offered good in vitro activity against T. rubrum (Table 1). All isolates were far more susceptible to the 3 newer triazoles than to itraconazole (Table 1) and comparable to those reported by other studies (7,9,10,14,17,18).Isavuconazole is a novel broad-spectrum triazole agent and has the same mechanism of action as the other tr...